| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151346796-151347076 | Rare:76 | ||||
| chr1:151347170-151347574 | Rare:93 | ||||
| chr1:151399230-151399283 | Common:6; Rare:12 | ||||
| chr1:151399339-151399638 | Common:3; Rare:89; Clinvar (pathogenic):2 | ||||
| chr1:151399957-151400022 | Rare:22 | ||||
| chr1:151400032-151400103 | Rare:16 | ||||
| chr1:151400135-151400180 | Rare:12 | ||||
| chr1:151455378-151455441 | Rare:10 | ||||
| chr1:151458701-151458866 | Common:3; Rare:103 | ||||
| chr1:151458868-151459007 | Rare:53 | ||||
| chr1:151459034-151459268 | Common:1; Rare:74 | ||||
| chr1:151459312-151459600 | Common:2; Rare:109 | ||||
| chr1:151510919-151510983 | Rare:12 | ||||
| chr1:151511086-151511417 | Common:4; Rare:77 | ||||
| chr1:151540129-151540419 | Common:1; Rare:98 |